Evidence map›Paper›PMID 30356717›Full record

ArticleFrontiers in immunology2018

Early IFNγ-Mediated and Late Perforin-Mediated Suppression of Pathogenic CD4 T Cell Responses Are Both Required for Inhibition of Demyelinating Disease by CNS-Specific Autoregulatory CD8 T Cells.

Alexander W Boyden, Ashley A Brate, Nitin J Karandikar

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Myelin-reactive CD8Journal of neuroinflammation · 2025
    Article
  4. Article
  5. A Functionally Distinct CXCR3Journal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Towards Clinical Translation of CD8International journal of molecular sciences · 2019
    Review
  11. Advances in the Study of CD8+ Regulatory T Cells.Critical reviews in immunology · 2019
    Review
  12. Review
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Alexander W BoydenDepartment of Pathology, University of Iowa, Iowa City, IA, United States.
Ashley A BrateDepartment of Pathology, University of Iowa, Iowa City, IA, United States.
Nitin J KarandikarDepartment of Pathology, University of Iowa, Iowa City, IA, United States.
Veterans Health Administration · USUniversity of Iowa · US

Funding

Immune Dysregulation During Multiple Sclerosis RelapseR01AI121567 · NIAID · UNIVERSITY OF IOWA · PI KARANDIKAR, NITIN J · 2016 to 2020
$3.8M
CNS-SPECIFIC REGULATORY CD8+ T CELLS IN AUTOIMMUNE DEMYELINATIONR01AI092106 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI KARANDIKAR, NITIN J · 2011 to 2015
$1.7M
Immunotherapeutic Regulatory CD8 T cells in Autoimmune Demyelinating DiseaseI01BX003677 · VA · IOWA CITY VA MEDICAL CENTER · PI KARANDIKAR, NITIN J · 2017 to 2025
–
BLRD VA I01 BX003677NIAID NIH HHS R01 AI092106NIAID NIH HHS R01 AI121567
6 · The paper itself

Abstract

Pathogenesis of immune-mediated demyelinating diseases like multiple sclerosis (MS) is thought to be governed by a complex cellular interplay between immunopathogenic and immunoregulatory responses. We have previously shown that central nervous system (CNS)-specific CD8 T cells have an unexpected protective role in the mouse model of MS, experimental autoimmune encephalomyelitis (EAE). In this study, we interrogated the suppressive potential of PLP178-191-specific CD8 T cells (PLP-CD8). Here, we show that PLP-CD8, when administered post-disease onset, rapidly ameliorated EAE progression, and suppressed PLP178-191-specific CD4 T cell responses as measured by delayed-type hypersensitivity (DTH). To accomplish DTH suppression, PLP-CD8 required differential production of perforin and IFNγ. Perforin was not required for the rapid suppressive action of these cells, but was critical for maintenance of optimal longer term DTH suppression. Conversely, IFNγ production by PLP-CD8 was necessary for swift DTH suppression, but was less significant for maintenance of longer term suppression. These data indicate that CNS-specific CD8 T cells employ an ordered regulatory mechanism program over a number of days

Indexed as

AnimalsAutoimmunityCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCytotoxicity, ImmunologicDemyelinating Autoimmune Diseases, CNSDisease Models, AnimalDisease ProgressionEncephalomyelitis, Autoimmune, ExperimentalImmunomodulationInterferon-gammaMiceMice, KnockoutMultiple SclerosisPerforinT-Cell Antigen Receptor SpecificityInterferon-gammaPerforinautoimmunityCD4 T cellsCD8 T cellsEAEinterferon-gammamultiple sclerosisperforinregulation

Identifiers

PMID30356717
PMCPMC6189364
OpenAlexW2895967090

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.